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dc.rights.licenseopenen_US
dc.contributor.authorLAFITTE, Marianne
dc.contributor.authorTASTET, Sandrine
dc.contributor.authorPEREZ, Paul
dc.contributor.authorSERISE, Marie-Aimee
dc.contributor.authorGRANDOULIER, Anne-Sophie
hal.structure.identifierNutrition et Neurobiologie intégrée [NutriNeuro]
dc.contributor.authorAOUIZERATE, Bruno
IDREF: 069471851
hal.structure.identifierInstitut de Neurosciences cognitives et intégratives d'Aquitaine [INCIA]
dc.contributor.authorSIBON, Igor
hal.structure.identifierNutrition et Neurobiologie intégrée [NutriNeuro]
dc.contributor.authorCAPURON, Lucile
IDREF: 167018736
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
dc.contributor.authorCOUFFINHAL, Thierry
dc.date.accessioned2021-09-01T08:49:34Z
dc.date.available2021-09-01T08:49:34Z
dc.date.issued2015-03-18
dc.identifier.issn1471-2261en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/110273
dc.description.abstractEnBACKGROUND: Major depression disorder (MDD) is a common condition in patients suffering from acute coronary syndrome (ACS), and depression is a risk factor for mortality following an ACS. Growing evidence suggests that there is an intricate interplay between atherosclerosis, inflammation and depression. The aim of this study was to investigate the role of atherosclerosis-induced inflammation in the mediation of MDD. METHODS: 87 patients without depression were recruited at the time of an ACS, evaluated at 3 and 7 days and followed at 1, 3 and 9 months for the occurrence of a MDD as assessed by structured interviews (MINI). At each time point, they were monitored for inflammatory markers (high sensitivity C Reactive Protein {hsCRP} and fibrinogen), cardiovascular risk factors and atherosclerosis burden. Association between possible predictive characteristics and depression was assessed using a multivariable logistic regression model. RESULTS: The overall incidence of MDD, in this population, was 28.7% [95% CI: 19.5 - 39.4] during the 9-month follow up period. Elevated hsCRP was not associated with depression onset after an ACS (adjusted OR: 1.07 [0.77 - 1.48]; p = 0.70), and similarly no association was found with fibrinogen. Furthermore, we found no association between hsCRP, fibrinogen or atherosclerosis burden at any time-point, and the occurrence of a MDD (or HDRS-17 and MADRS). The only factor associated with depression occurrence after an ACS was a previous personal history of depression (adjusted OR: 11.02 [2.74 to 44.34]; p = 0.0007). CONCLUSIONS: The present study shows that after an ACS, patients treated with optimal medications could have a MDD independent of elevated hsCRP or fibrinogen levels. Personal history of depression may be a good marker to select patients who should be screened for depression after an ACS.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enAcute Coronary Syndrome
dc.subject.enAdult
dc.subject.enAged
dc.subject.enBiomarkers
dc.subject.enC-Reactive Protein
dc.subject.enCoronary Artery Disease
dc.subject.enDepressive Disorder
dc.subject.enMajor
dc.subject.enFemale
dc.subject.enFibrinogen
dc.subject.enHumans
dc.subject.enMale
dc.subject.enMiddle Aged
dc.subject.enPrognosis
dc.subject.enRisk Factors
dc.title.enHigh sensitivity C reactive protein, fibrinogen levels and the onset of major depressive disorder in post-acute coronary syndrome
dc.typeArticle de revueen_US
dc.identifier.doi10.1186/s12872-015-0015-3en_US
dc.subject.halSciences du Vivant [q-bio]/Neurosciences [q-bio.NC]en_US
dc.identifier.pubmed25888123en_US
bordeaux.journalBMC Cardiovascular Disordersen_US
bordeaux.page23en_US
bordeaux.volume15en_US
bordeaux.hal.laboratoriesNutriNeurO (Laboratoire de Nutrition et Neurobiologie Intégrée) - UMR 1286en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINRAEen_US
bordeaux.institutionINSERM
bordeaux.teamPsychoneuroimmunologie et Nutrition: Approches expérimentales et cliniquesen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.exportfalse
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=BMC%20Cardiovascular%20Disorders&rft.date=2015-03-18&rft.volume=15&rft.spage=23&rft.epage=23&rft.eissn=1471-2261&rft.issn=1471-2261&rft.au=LAFITTE,%20Marianne&TASTET,%20Sandrine&PEREZ,%20Paul&SERISE,%20Marie-Aimee&GRANDOULIER,%20Anne-Sophie&rft.genre=article


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